rs111033482

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs111033482(A;C)

Make rs111033482(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77189373

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033482
dbSNP (classic)	rs111033482
ClinGen	rs111033482
ebi	rs111033482
HLI	rs111033482
Exac	rs111033482
Gnomad	rs111033482
Varsome	rs111033482
LitVar	rs111033482
Map	rs111033482
PheGenI	rs111033482
Biobank	rs111033482
1000 genomes	rs111033482
hgdp	rs111033482
ensembl	rs111033482
geneview	rs111033482
scholar	rs111033482
google	rs111033482
pharmgkb	rs111033482
gwascentral	rs111033482
openSNP	rs111033482
23andMe	rs111033482
SNPshot	rs111033482
SNPdbe	rs111033482
MSV3d	rs111033482
GWAS Ctlg	rs111033482

Max Magnitude

0

ClinVar
Risk	rs111033482(C;C)
Alt	rs111033482(C;C)
Reference	Rs111033482(A;A)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76900418A>C
CLNSRC	ClinVar
CLNACC	RCV000036114.2,